KLOR-CON

Product NDC
0615-8045
11-digit product format
006158045
Labeler code
0615
Product ID
0615-8045_be902110-883c-4fc5-b197-ee3a10286eec
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
potassium chloride
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
NDA019123
Marketing category
NDA
Marketing start
2014-09-01
Marketing end
2021-06-30
Substance
POTASSIUM CHLORIDE
Active strength
750 mg/1
Pharmacologic classes
Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0615-8045-050061580450515 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8045-05) 2016-04-132021-06-30NoNoCurrent
0615-8045-140061580451414 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8045-14) 2017-08-082021-06-30NoNoCurrent
0615-8045-390061580453930 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8045-39) 2016-04-132021-06-30NoNoCurrent